Xiong Yan, Lu Xiaoxue, Li Bohao, Xu Shiyao, Fu Beibei, Sha Zhou, Tian Rong, Yao Rui, Li Qian, Yan Jingmin, Guo Dong, Cong Zixuan, Du Yongliang, Lin Xiaoyuan, Wu Haibo
School of Life Sciences, Chongqing University, Chongqing, 401331, China.
Department of Clinical Microbiology and Immunology, College of Pharmacy and Medical Laboratory, Army Medical University (Third Military Medical University), Chongqing, 400038, China.
Adv Sci (Weinh). 2025 Mar;12(9):e2409740. doi: 10.1002/advs.202409740. Epub 2025 Jan 13.
The diverse and dynamic population of microorganisms present in the gut microbiota may affect host health. There are evidences to support the role of gut microbiota as a key player in reproductive development. Unfortunately, the relationship between reproductive disorders caused by aging and gut microbiota remains largely unknown. Here, it is shown for the first time that gut microorganism Bacteroides fragilis (BF) transplantation ameliorates ovarian aging by transporting extracellular vesicles (EVs) through the gut-ovary axis. Mechanistically, miR-1246 is enriched in EVs derived from BF-treated intestinal cells, and these miR-1246-enriched EVs are transferred to ovaries, thereby effectively improving reproductive senescence by reducing oxidative stress in the ovaries. Specifically, miR-1246 reduces the ubiquitination of p62 and stabilizes the protein level of p62 by targeting E3 ligase SKP2. Then Keap1-Nrf2 complex is dissociated and Keap1 is recruited to form the p62-Keap1 complex. With the dissociation of Keap1-Nrf2 complex, Nrf2 is released and activated, thus promoting the transcription of antioxidant enzymes and relieving reproductive senescence. Collectively, the data indicates that intestinal cell-derived EVs serve as natural information carriers in the crosstalk between the gut and the ovary, and intestinal microorganism transplantation is a promising approach for the treatment of ovarian dysfunction diseases.
肠道微生物群中存在的多样且动态的微生物群体可能会影响宿主健康。有证据支持肠道微生物群在生殖发育中起关键作用。不幸的是,衰老引起的生殖障碍与肠道微生物群之间的关系在很大程度上仍然未知。在此,首次表明肠道微生物脆弱拟杆菌(BF)移植通过肠道-卵巢轴转运细胞外囊泡(EVs)来改善卵巢衰老。从机制上讲,miR-1246在BF处理的肠道细胞衍生的EVs中富集,这些富含miR-1246的EVs被转移到卵巢,从而通过降低卵巢中的氧化应激有效地改善生殖衰老。具体而言,miR-1246通过靶向E3连接酶SKP2减少p62的泛素化并稳定p62的蛋白质水平。然后Keap1-Nrf2复合物解离,Keap1被募集形成p62-Keap1复合物。随着Keap1-Nrf2复合物的解离,Nrf2被释放并激活,从而促进抗氧化酶的转录并缓解生殖衰老。总体而言,数据表明肠道细胞衍生的EVs在肠道与卵巢之间的串扰中作为天然信息载体,并且肠道微生物移植是治疗卵巢功能障碍疾病的一种有前景的方法。